Cancer
Acute Lymphoblastic Leukemia (ALL) |
Childhood Acute Lymphoblastic Leukemia |
Childhood Leukemia |
Erythrocytosis |
JAK2 V617F mutation |
Myelodysplastic Syndrome |
Myeloproliferative Disorder |
Peripheral T cell lymphoma |
Polycythemia Vera |
Acute Lymphoblastic Leukemia (ALL) |
Childhood Acute Lymphoblastic Leukemia |
Childhood Leukemia |
Erythrocytosis |
JAK2 V617F mutation |
Myelodysplastic Syndrome |
Myeloproliferative Disorder |
Peripheral T cell lymphoma |
Polycythemia Vera |
Arginine-succinic aciduria |
Atherosclerosis (hyperlipidemia) |
Benefit of Niacin in Reducing Lipoprotein (a) |
Cardiovascular Disease (Cholesterol Level) |
Dysfunctional HDL |
Familial Hyperlipoproteinemia Type III |
Hereditary familial hypercholesterolemia |
Hypercholesterolemia (Type B) |
Jervell and Lange-Nielsen Syndrome |
Narrowing of Blood Vessels (Stenosis) |
Platelets (Highest Count) |
Platelets (Lowest Count) |
Prothrombin (G20210A Mutation) |
Pulmonary Embolism |
Venous Thromboembolism (VTE) |
Homocysteine Accumulation |
Lipoprotein (a) |
Response to Clopidogrel |
Fasting Glucose Level Increase |
Gilbert’s Syndrome |
ALT / AST Index |
A1 A2 Alloantigen Polymorphism |
Alpha Antitrypsin Deficiency (AAT) |
Alpha-2-Macroglobulin Polymorphism |
Cholesterol Ester Transfer Protein Deficiency |
Elliptocytosis |
Factor II Deficiency (Prothrombin) |
Factor VII Protease Polymorphism (Marburg) |
Gamma-Glutamylcysteine Synthetase Deficiency |
Glutathione Synthetase Deficiency |
Hereditary angioedema |
Hyperimmunoglobulin E (Hyper IgE) Syndrome |
Leukocyte Adhesion Deficiency – Type 1 |
Mevalonate Kinase Deficiency |
Multiple Sulphatase Deficiency (Austin’s Disease) |
OKT4 deficiency |
Upshaw Schulman Syndrome |
Von Willebrand Disease |
Wiskott-Aldrich Syndrome |
Activated partial thromboplastin time (aPTT) |
Afibrinogenemia |
Albumin |
Alpha-Defensins Levels |
Argininemia |
Aspartate Aminotransferase (AST) |
Atypical Hemolytic Uremic Syndrome (aHUS) |
Benefit of Physical Exercise for HDL |
Beta Thalassemia |
Bilirubin |
Bleeding Disorder (Platelets) |
Blood Glucose Level |
Carbamoyl Phosphate Synthetase I Deficiency |
Circulating Glycated Hemoglobin (HbA1c) |
Congenital Dyserythropoietic Anemia |
Congenital Thrombotic Thrombocytopenic Purpura |
Congenital afibrinogenemia |
Crigler-Najjar Syndrome |
D-dimers (Fibrin Degradation Products) |
Deficiency of Vitamin K-Dependent Coagulation Factors |
Essential Thrombocythemia |
Excess Calcium in Blood |
Factor V deficiency |
Factor VII Deficiency |
Factor XII Polymorphism |
Factor XIII deficiency |
Fanconi’s anemia |
G6PD deficiency |
Galactose Epimerase Deficiency |
Glanzmann’s thrombasthenia |
HDL (Cholesterol) |
HDL Deficiency (Family) |
Haptoglobin |
Hemochromatosis |
Hemolytic Anemia |
Hemophilia – Factor VIII Deficiency |
Hemophilia A |
Hemophilia B |
Hereditary Persistence of Fetal Hemoglobin (HPFH) |
Hereditary Stomatocytosis |
High Ferritin |
High ferritin (in men) |
Higher HDL on Low Carbohydrate Diets |
Hyperbilirubinemia |
Hyperhomocysteinemia |
Hypoproteinemia |
Idiopathic Hypereosinophilic Syndrome |
Intermediate Beta Thalassemia |
L-ferritin deficiency |
LDL (Cholesterol) |
Low Ferritin in Men |
Low Ferritin in Women |
Low ferritin in children under 2 years |
Lower Hemoglobin Levels |
Microcytic Anemia |
Neuroferritinopathy |
Ornithine Transcarbamylase Deficiency |
Oxidized LDL |
Paroxysmal Nocturnal Hemoglobinuria (PNH) |
Platelet Count |
Post-Transfusion Purpura (PPT) |
Reduction in Factor VIII Activity (Coagulation) |
Reduction in Factor XII Activity (Coagulation) |
Shwachman-Diamond Syndrome |
Sickle cell anemia |
Spherocytosis |
TIBC |
Tendency to have Increased Eosinophils in Contact with Allergens |
Thiamine-Responsive Megaloblastic Anemia |
Thrombocytopenia |
Thrombophilia (Factor V – Protein C) |
Thrombophilia (Factor VII) |
Transferrin |
Triglycerides |
Villejuif Hemoglobin |
X Factor Deficiency |
Hereditary Sideroblastic Anemia |
Hepcidin |
Anti-Beta-2-Glycoprotein Antibody |
Anti-DNA Antibody |
Anticardiolipin Antib. |
Antiphospholipid Antibody Syndrome |
Antithrombin Deficiency |
Autoimmune Lymphoproliferative Syndrome (ALPS) |
Congenital Erythropoietic Porphyria (Gunther’s Disease) |
Factor V Leiden Mutation |
Familial hemophagocytic lymphohistiocytosis (HLH) |
Human Leukocyte Antigen (HLA) |
Lupus |
Lupus anticoagulant |
Malaria Resistance |
Mannose Binding Protein Deficiency |
Mutation of the SERPINE1 Gene (PAI-1) |
Phenylketonuria |
Primary Functional Neutrophil Disorder |
Prolactin Promoter Polymorphism |
Protein C Deficiency |
Protein S Deficiency |
Resistance to HIV (AIDS) |
Resistance to Norovirus (NoV) |
Type 2 X-linked Lymphoproliferative Syndrome |
Wegener’s granulomatosis |
X-linked Lymphoproliferative Syndrome (XLP) |
Ceruloplasmin |
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency |
Greater Insulin Sensitivity with Physical Exercise |
Lactate dehydrogenase (LDH) |
Methionine Adenosyltransferase Deficiency |
Cobalamin Intracellular Metabolism Disease |
Dyslipidemia |
Galactosemia |
Homocystinuria |
Hyperferritinemia |
Low Ferritin |
Myoadenylate Deaminase Deficiency |
MTHFR rs1801131 |
MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) |
MTHFR rs1801133 |
Betaine |
Iron |
Toxic Sensitivity to Benzene |
Warfarin |
Aspergillosis |
Oxygen Volume (O2) Max (VO2 Max) |
Basal Blade Disease |
Erythropoietic Protoporphyria |
Hyperchromias |
Gout |
Hematuria |
Uric Acid (Concentration) |
Vitamin B3 (Niacin) |